A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18933



Internal ID15481407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:134861..135297hg38UCSC Ensembl
Outerchr10:134401..137561hg38UCSC Ensembl
Innerchr10:180801..181237hg19UCSC Ensembl
Outerchr10:180341..183501hg19UCSC Ensembl
Innerchr10:170801..171237hg18UCSC Ensembl
Outerchr10:170341..173501hg18UCSC Ensembl
Innerchr10:170801..171237hg17UCSC Ensembl
Outerchr10:170341..173501hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383161
hg193161
hg183161
hg173161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8594
Supporting Variants
SamplesNA07048
Known GenesZMYND11
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv18933
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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